5C56.21
category
Oligosaccharidosis
Also indexed as
Adult alpha-mannosidosisAdult-onset Alpha-N-acetylgalactosaminidase deficiencyAlpha-L-fucosidase deficiencyAlpha-N-acetylgalactosaminidase deficiencyAlpha-N-acetylgalactosaminidase deficiency type 1Alpha-N-acetylgalactosaminidase deficiency type 2Alpha-N-acetylgalactosaminidase deficiency type 3Alpha-mannosidosisAspartylglucosaminidase deficiencyAspartylglucosaminuriaBeta-mannosidosisCherry-red-spot-myoclonus syndromeCombined deficiency of neuraminidase and beta-galactosidaseCongenital sialidosis type 2FucosidosisGalactosialidosisGoldberg syndromeInfantile alpha-mannosidosisInfantile dysmorphic sialidosisJuvenile sialidosis type 2Kanzaki diseaseLipomucopolysaccharidosisLysosomal alpha-D-mannosidase deficiencyLysosomal beta-mannosidase deficiencyMannosidosis, not otherwise specifiedMucolipidosis type 1N-acetyl-alpha-D-galactosaminidase deficiencyNAGA - [Alpha-N-acetylgalactosaminidase] deficiencyNAGA deficiency type 1 - [Alpha-N-acetylgalactosaminidase deficiency type 1]NAGA deficiency type 2 - [Alpha-N-acetylgalactosaminidase deficiency type 2]NAGA deficiency type 3 - [Alpha-N-acetylgalactosaminidase deficiency type 3]Neuraminidase deficiency with beta-galactosidase deficiencyNormomorphic sialidosisOligosaccharidosisProtective protein deficiencySchindler diseaseSchindler disease type 1Schindler disease type 2Schindler disease type 3SialidosisSialidosis type 1Sialidosis type 2mannosidase deficiency